Speakers-2019 – Abilities Days
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Ιωάννης Βαρβάκης - Βικιπαίδεια
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
A novel familial mutation associated with Treacher Collins syndrome: A case report
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report | Makarios Eleftheriades - Academia.edu
Ioannis Papoulidis - Senior Funds Accountant - Alter Domus | LinkedIn
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
Loop | IOANNIS PAPOULIDIS
Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search | Molecular Cytogenetics | Full Text
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Best Practices in PGT 2019 – Embryolab Academy
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
Γιάννης Παπουλίδης (@JonAPap) / Twitter
Ο Διευθυντής του εργαστηρίου... - ATG - Access To Genome | Facebook
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male | Molecular Cytogenetics | Full Text
Molecular Cytogenetics Research Papers - Academia.edu
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) – topic of research paper in Clinical medicine. Download scholarly article PDF and read for
